Method for heteroepitaxial growth of high-quality N-face GaN, InN, and AlN and their alloys by metal organic chemical vapor deposition

ABSTRACT

Methods for the heteroepitaxial growth of smooth, high quality films of N-face GaN film grown by MOCVD are disclosed. Use of a misoriented substrate and possibly nitridizing the substrate allow for the growth of smooth N-face GaN and other Group III nitride films as disclosed herein. The present invention also avoids the typical large (μm sized) hexagonal features which make N-face GaN material unacceptable for device applications. The present invention allows for the growth of smooth, high quality films which makes the development of N-face devices possible.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of the following commonly-assigned U.S. patent application:

U.S. patent application Ser. No. 11/855,591, filed on Sep. 14, 2007, by Stacia Keller, Umesh K. Mishra, and Nicholas A. Fichtenbaum, entitled “METHOD FOR HETEROEPITAXIAL GROWTH OF HIGH-QUALITY N-FACE GaN, InN, AND AIN AND THEIR ALLOYS BY METAL ORGANIC CHEMICAL VAPOR DEPOSITION,”; now U.S. Pat. No. 7,566,580, issued Jul. 28, 2009, which application claims the benefit under 35 U.S.C. Section 119(e) of U.S. Provisional Application Ser. No. 60/866,035 filed on Nov. 15, 2006, by Stacia Keller, Umesh K. Mishra, and Nicholas A. Fichtenbaum, entitled “METHOD FOR HETEROEPITAXIAL GROWTH OF HIGH-QUALITY N-FACE GaN, InN, AND AlN AND THEIR ALLOYS BY METAL ORGANIC CHEMICAL VAPOR DEPOSITION,” ;

which applications are incorporated by reference herein.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT

This invention was made with Government support under Grant No. N00014-05-1-0419, awarded by ONR DARPA MINE. The Government has certain rights in this invention.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention is related to growth of Group III nitride materials, and in particular to a method of heteroepitaxial growth of high quality, Nitrogen (N) face Gallium Nitride (GaN), Indium Nitride (InN), Aluminum Nitride (AlN), and their alloys, by Metal Organic Chemical Vapor Deposition (MOCVD).

2. Description of the Related Art

(Note: This application references a number of different publications as indicated throughout the specification by one or more reference numbers within brackets, e.g., [x]. A list of these different publications ordered according to these reference numbers can be found below in the section entitled “References.” Each of these publications is incorporated by reference herein.)

The use of group III nitride materials in consumer applications and devices is becoming widespread. However, the majority of applications employ Ga-polar group-III nitride films and heterostructures. Films and heterostructures of the opposite polarity (N-polar group-III nitride films and heterostructures) have been much less investigated due to difficulties in their growth. N-polar group-III nitride films and heterostructures are advantageous for the fabrication of a variety of nitride based electronic and optoelectronic devices. The opposite direction of the piezoelectric fields in N-polar heterostructures, in comparison to Ga-polar heterostructures, allows the fabrication of transistor devices which cannot be fabricated using Ga-polar heterostructures.

One of the major challenges to III-Nitride based light emitters is the growth of high quality InGaN with high In composition. The use of the Gallium (Ga)-face for devices limits the temperature at which the InGaN can be grown, which limits the types of devices that can be made. Another challenge is the growth of low resistance p-type (Al, Ga, In)N:Mg films due to polarity conversion from Ga-face to N-face at high Mg doping levels. By using N-face (Al, Ga, In)N layer structures both issues can be mitigated.

The opposite direction of the piezoelectric fields in N-polar in comparison to Ga-polar heterostructures leads to a lower operating voltage of Light Emitting Diodes (LEDs) and Laser Diodes (LDs), and to improved carrier injection in p-n junction devices, due to a narrower width of the depletion region in general. Furthermore, the opposite direction of the piezoelectric fields has advantages for devices such as transistors, solar cells and devices utilizing tunnel junctions. It can be seen that there is a need in the art for N-face nitride materials and methods to grow these materials.

SUMMARY OF THE INVENTION

The present invention describes growth of Group III nitride materials, and in particular a method of heteroepitaxial growth of high quality, N-face GaN, InN, AlN, and their alloys, and heterostructures comprising the same grown by MOCVD.

A method for growing an N-face group III nitride film in accordance with the present invention comprises providing a substrate having a growth surface with a misorientation angle between 0.5 and 10 degrees in any direction relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices; and growing the N-face group III-nitride film on the growth surface, wherein the group III-nitride film having an N-face is smoother than an N-face group III-nitride film grown on a substrate without a misorientation angle.

If sapphire is used as substrate, such a method further optionally comprises a misorientation of the [0001] sapphire with a direction of <11-20>, the miller indices of the misorientation direction are h=1, i=1, k=−2 and l=0 or equivalent. If the substrate is [000-1] C-face silicon carbide, such a method optionally comprises a misorientation with a misorientation direction of <1-100>, the miller indices of the misorientation direction are h=1, i=−1, k=0 and l=0 or equivalent. If the substrate is [111] silicon, such a method optionally comprises a misorientation with a misorientation direction of <−1-12>, the miller indices of the misorientation direction are h=−1, k=−1 and l=2 or equivalent, or a misorientation direction of <11-2>, the miller indices of the misorientation direction are h=1, k=1 and l=−2 or equivalent.

Such a method can further optionally comprise the growing being by Metal Organic Chemical Vapor Deposition (MOCVD), the group III-nitride layer having an N-face being grown on a nitridized misoriented substrate, forming an AlN layer on the misoriented substrate and growing the group III-nitride layer having an N-face on the AlN layer, the AlN layer being deposited using a step flow growth mode, the AlN layer setting an N-polarity for subsequently deposited group III-nitride layers, the misoriented substrate being a sapphire substrate, depositing a group III-nitride nucleation layer on an AlN layer formed on the sapphire substrate due to the nitridization, and growing the main group III-nitride layer on the group III-nitride nucleation layer, the group III-nitride nucleation layer being deposited using a step flow growth mode or layer by layer growth mode, the group III-nitride nucleation layer being at least partially doped, the growing of the group III-nitride layer having an N-face comprises doping and growing, on the nucleation layer, a first group III nitride layer having an N-face, using a low ammonia partial pressure and growing a second group III-nitride layer having an N-face, on the first group-III layer having an N-face, at a high ammonia partial pressure, so that at least part of the second group III-nitride layer having an N-face is doped, the misoriented substrate being a polished Carbon Polar Silicon Carbide substrate, and depositing a graded or stepped group III-nitride layer, e.g., the layer has a changing composition of one of the elements used to make up the layer, on the AlN layer, wherein an Al composition of the graded or stepped group III-nitride layer is graded or stepped from AlN to GaN.

Additional optional items in accordance with the present invention include the graded group III-nitride layer is at least partially doped, the growing of the group III-nitride layer having an N-face comprises doping and growing, on the graded group III-nitride layer, a first group III-nitride layer having an N-face, using a low ammonia partial pressure, and growing a second group III-nitride layer having an N-face, at a high ammonia partial pressure, so that at least part of the second group III-nitride layer having an N-face is doped, and a device fabricated using the method.

Another method for creating a group III-nitride film with an abrupt p-type doping profile in accordance with the present invention comprises providing a substrate having a growth surface with a misorientation angle between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices; and growing the N-face group III-nitride film having an abrupt p-type doping profile on the growth surface, wherein the group III-nitride film having an N-face is smoother than an N-face group III-nitride film grown on a substrate without a misorientation angle.

Another method for enhancing charge transport properties of a nitride device in accordance with the present invention comprises fabricating the nitride device using N-face nitride layers grown on a substrate having a growth surface with a misorientation angle between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices, and aligning a channel of the nitride device substantially perpendicular to a misorientation direction of the misoriented (Al, Ga, In)N epitaxial layer, wherein charge transport properties are enhanced perpendicular to the misorientation direction.

BRIEF DESCRIPTION OF THE DRAWINGS

Referring now to the drawings in which like reference numbers represent corresponding parts throughout:

FIG. 1 illustrates a process chart in accordance with the present invention, for the growth on sapphire.

FIG. 2A illustrates a process chart in accordance with the present invention, for the growth on silicon carbide.

FIG. 2B illustrates a process chart in accordance with the present invention, for the growth on silicon.

FIG. 3 illustrates a process chart in accordance with the present invention, for the growth of semi-insulating GaN on sapphire.

FIG. 4A illustrates a process chart in accordance with the present invention, for the growth of semi-insulating GaN on silicon carbide substrate.

FIG. 4B illustrates a process chart in accordance with the present invention, for the growth of semi-insulating GaN on a silicon (111) substrate.

FIG. 5( a) shows an optical microscope image of an N-face GaN film grown by MOCVD on a nitrided sapphire substrate, and FIG. 5( b) shows an atomic force microscope (AFM) image of N-face GaN grown by MOCVD on a nitrided sapphire substrate

FIG. 6 shows transmission electron micrographs, under different imaging conditions, of an N-face GaN film grown using the present invention

FIG. 7( a) shows an AFM image of InGaN/GaN multi quantum wells (MQWs) grown using the present invention, and FIG. 7( b) shows photoluminescence (PL) from MQWs comprising 5×(3 nm thick In_(0.1)Ga_(0.9)N/8 nm thick GaN).

FIG. 8 shows X-ray Diffraction (XRD) of N-face nitride MQWs comprising 5×(4 nm thick In_(0.12)Ga_(0.88)/10 nm thick GaN).

FIG. 9 is a graph showing SIMS results of oxygen impurities as a function of temperature.

FIG. 10 is a graph showing SIMS results of carbon impurities as a function of temperature.

FIGS. 11( a) and 11(b) are graphs of SIMS results of Mg incorporation in an N-face (FIG. 11( a)) and a Ga-face (FIG. 11( b)) GaN SIMS stack.

FIGS. 12 a-12 f illustrate optical micrographs of 0.8 micron thick GaN films grown on sapphire substrates in accordance with the present invention.

FIG. 13 illustrates one or more embodiments of the present invention that incorporate growth of additional III-nitride films.

FIGS. 14A-14C illustrate micrographs of N-polar films grown on various substrates in accordance with one or more embodiments of the present invention.

FIGS. 15A-B illustrate micrographs of the GaN surface showing surface topologies.

FIGS. 16A-B illustrate micrographs of a GaN film produced in one or more embodiments of the present invention.

FIG. 17 illustrates one or more embodiments of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

In the following description of the preferred embodiment, reference is made to the accompanying drawings which form a part hereof, and in which is shown by way of illustration a specific embodiment in which the invention may be practiced. It is to be understood that other embodiments may be utilized and structural changes may be made without departing from the scope of the present invention.

Overview

This invention will allow for the creation of transistors that cannot be fabricated on traditional Ga-polar GaN. The present invention will also allow novel polarization-based band structure designs to create more efficient LEDs and LDs. The reverse polarization fields in N-polar heterostructures, in comparison to Ga-polar heterostructures, result in lower operating voltages, shrink the width of the depletion region of the p-n-junction, and improve carrier injection, leading to advances in device performance. Deposition on N-polar surfaces enables the growth of InGaN with higher compositions of Indium compared to Ga-polar surfaces, easing the push of LED wavelengths into the yellow and red portions of the color spectrum. Additionally, the present invention enables the use of higher p-type doping levels in GaN based devices, leading to improved device performance. Further, novel electronic and optoelectronic nitride devices such as N-face transistors (HEMTs), N-face LEDs, and N-face LDs, will be possible using the materials grown using the present invention.

This invention enables the heteroepitaxial growth of high quality, smooth N-face (000-1) InN, GaN, AlN films, and their alloys, by MOCVD. Since free standing GaN substrates are not readily available and affordable, GaN is usually grown heteroepitaxially on Silicon Carbide (SiC), Sapphire, Si, and various other substrates.

The group III-Nitrides have large built-in polarization fields centered about the [0001] direction which makes the direction, and hence face of growth, an extremely important parameter in the growth and design of devices. Traditionally all III-Nitride growth is performed on the (0001) III-face. Since this invention allows N-face growth, new transistor (HEMTs), LEDs and LDs designs will be possible through the different physical properties provided by N-face. For HEMTs, the (000-1) N-face allows, for example, the design of structures with extremely low gate leakages for high power, high frequency device operation. For light emitters (LEDs, and LDs) the N-face enables the growth of better quality, high Indium composition InGaN alloys, which are currently needed to create high power devices in the green, yellow, and red parts of the color spectrum. Additionally, traditional Ga-face GaN suffers from inversion, while N-face GaN does not, when doped highly with Mg, which is need to create p-type GaN. Higher p-type carrier concentrations should drastically increase device performances. Moreover, the reverse polarization fields in N-face in comparison to Ga-face heterostructures lower the operating voltage of LEDs and LDs. This also results in a narrower width of the depletion region of the p-n-junction and improved carrier injection leading to advances in the device performance.

Whereas smooth N-face GaN films can be easily obtained on C-face SiC substrates using Molecular Beam Epitaxy (MBE) as growth techniques, films grown by MOCVD typically exhibit rough surfaces caused by the formation of hexagonal hillocks, independent of whether the GaN layers were grown on small GaN single crystals or on foreign substrates, hampering the development of N-face devices. [1, 2, 3] However, investigations on GaN single crystals showed that the hillock formation can be largely suppressed if the MOCVD growth is performed on miscut GaN crystals [2, 3]. More recently, smooth N-face GaN films were also obtained on sapphire substrates by Matsuoka et al. [4].

The present invention utilizes a misoriented substrate, for example (0001) sapphire or (000-1) SiC, which are misoriented for example in the <1-100> or <11-20> direction in order to obtain smooth N-face films grown by MOCVD. Thereby the technique can be applied to any foreign substrate, e.g., sapphire, SiC or Si.

Thereby, for growth on sapphire, the preferred substrate misorientation direction is <11-20>, leading to group-III nitride surface steps and/or undulations parallel to the <11-20> direction of the GaN crystal. For growth on carbon-polar silicon carbide, the preferred substrate misorientation direction is <1-100>, also leading to group-III nitride surface steps and/or undulations parallel to the <11-20> direction of the GaN crystal.

The preferred misorientation angle ranges between 1-5 degrees relative to a miller indexed surface [h, i, k, l] of the substrate, where h, i, k, l are miller indices. All misorientation angles and directions are given with respect of either the (0001) (=c-plane) sapphire surface (=plane) or the (000-1) SiC substrate surface. Both are suitable for the growth of (000-1) GaN. The present invention can also work for the growth of other N-terminated GaN planes on other substrate planes.

TECHNICAL DESCRIPTION

Growth on Sapphire

For growth on sapphire, the present invention is realized by:

a. Placing a misoriented sapphire substrate in the MOCVD reactor and annealing at around 1090° C. surface temperature in a H₂ environment.

b. The substrate is then nitridized in NH₃ and H₂ for several seconds at approximately 980° C. surface temperature, leading to the formation of a thin AlN layer on the sapphire which sets the N-face polarity of the growth.

c. NH₃ and Trimethylgallium (TMG) are then flowed into the reactor to commence growth of GaN on the AlN. Thereby, first an about 20 nm thick GaN layer can be deposited at medium growth temperatures (surface temperature ˜950° C.), leading to growth in a step-flow or layer-by-layer growth mode.

d. NH₃ and Trimethylgallium (TMG) are then flowed into the reactor to commence growth of the main GaN on the layer formed in step (c).

Currently, the growth method being used is MOCVD; however this invention could become quite useful for other growth methods such as MBE, Hydride Vapor Phase Epitaxy (HVPE), and Chemical Beam Epitaxy (CBE), etc.

The process described in part (c) applies very generally to GaN growth. However, the invention can be easily utilized to create InN (with the use of TMI), AlN (with the use of TMA), or any of their alloys, also with other group-V atoms (Al, Ga, In)(N, P, As), by combining the appropriate precursors.

Other precursors can be used such as triethylgallium, triethylaluminum for group-III sources, and dimethylhydrazine for N sources. Any appropriate substrate can be used, such as SiC, Si, spinel, etc. The nitridation temperature and time can be varied, or completely eliminated, dependent on the substrate. Other growth initiation procedures can be applied. For example, the growth can be initiated with the deposition of an AlN layer etc., or no growth initiation step might be required at all. Note that, while part (b) specifies the deposition of a thin AlN layer, any thickness of the AlN layer may be used, and nitride materials other than AlN may be used. The annealing of the substrate can be eliminated. The substrate can be misoriented not only towards the <11-20> and <1-100> directions, but also in any other direction. Instead of a single composition layer, the composition of the layer/crystal can be modified for all individual growth steps. The growth of each individual layer may also be interrupted for the deposition of layers comprised of other materials, for example silicon nitride or silicon oxide, possibly for strain or dislocation management.

FIG. 1 illustrates a process chart in accordance with the present invention.

Block 100 represents the step of placing a misoriented sapphire substrate in a MOCVD chamber.

Block 102 represents the step of annealing the misoriented sapphire substrate.

Block 104 represents the step of nitridizing the annealed misoriented sapphire substrate to form a thin AlN surface layer to set an N-polarity for following group III nitride layers. [7, 8] Reference 7 describes the formation of the AlN layer, reference 8 is a theoretical calculation with the result that the AlN layer should be one bi-layer thick, corresponding to ˜0.5 nm.

Block 106 represents the step of depositing, on the AlN surface layer, a group III nitride nucleation layer in a step-flow or layer-by-layer growth mode.

Block 108 represents the step of growing the main group III nitride layer on the nucleation layer.

Growth on Carbon Polar SiC

For growth on carbon (C) polar SiC, this invention is realized by:

a. Placing a misoriented, polished (e.g. chemo-mechanically polished) C-polar SiC substrate in the MOCVD reactor and annealing at around 1090° C. surface temperature in a H₂ environment.

b. NH₃ and Trimethylaluminum (TMA) are then flowed into the reactor to commence growth of a thin AlN layer in a step-flow-growth-mode or layer-by-layer growth mode. To increase the surface mobility of Al-species, a surfactant, for example indium, in form of trimethylindium (TMI), can be additionally flowed into the reactor [5].

c. Trimethylgallium (TMG) is then also optionally flowed into the reactor to commence the growth of a graded or stepped Al_(x)Ga_(1-x)N layer, the composition of which is graded or stepped from AlN to GaN. The injection of TMI can be continued to ensure a step-flow-growth-mode or layer-by-layer growth mode of the layer.

d. NH₃ and Trimethylgallium are then flowed into the reactor to commence growth of the main GaN layer.

Currently, the growth method being used is MOCVD; however this invention could become quite useful for other growth methods such as MBE, HVPE, CBE, etc.

The process described in part (c) applies very generally to GaN growth however, the invention can be easily utilized to create InN (with the use of TMI), AlN (with the use of TMA), or any of their alloys, also with other group-V atoms (Al, Ga, In)(N, P, As), by combining the appropriate precursors. Other precursors can be used such as triethylgallium, triethylaluminum for group-III sources, and dimethylhydrazine for N sources. Any appropriate substrate can be used, such as SiC, Si, spinel, etc. The nitridation temperature and time can be varied, or completely eliminated, dependent on the substrate. Other growth initiation procedures can be applied. For example, the growth can be initiated with the deposition of an AlGaN layer etc., or no growth initiation step might be required at all. Note that, while part (b) specifies the deposition of a thin AlN layer, any thickness of the AlN layer may be used, and nitride materials other than AlN may be used. The annealing step of the substrate can be eliminated. The graded or stepped AlGaN layer can be eliminated and be replaced by any (Al, Ga, In)N layer of any composition if grown in a step-flow-growth-mode or layer-by-layer-growth-mode. The substrate can be misoriented not only towards the <1-100> or <11-20> directions but also in any other direction. Instead of a single composition layer, the composition of the layer/crystal can be modified for all individual growth steps. The growth of each individual layer may also be interrupted for the deposition of layers comprised of other materials, for example silicon nitride or silicon oxide, possibly for strain or dislocation management.

FIG. 2A illustrates a process chart in accordance with the present invention.

Block 200 represents the step of placing a misoriented, chemo-mechanically polished C-polar SiC substrate in a MOCVD chamber.

Block 202 represents the step of annealing the misoriented SiC substrate.

Block 204 represents the step of depositing, on the annealed misoriented substrate, a thin AlN layer in a step-flow or layer-by-layer growth mode.

Block 206 represents the optional step of introducing an additional Ga-precursor into the MOCVD chamber to deposit, on the AlN, a layer where the Al-composition is graded or stepped from AlN to GaN in a step-flow or layer by layer growth mode.

Block 208 represents the step of growing the main group III nitride layer on the graded layer.

Growth on Si

For growth on Si (111), this invention is realized by:

Placing a misoriented, polished (e.g. chemo-mechanically polished) Si (111) substrate in the MOCVD reactor and annealing at around 1090° C. surface temperature in a H₂ environment.

The substrate is then nitridized in NH₃ and H₂ for several seconds at approximately 980° C. surface temperature, leading to the formation of a thin silicon nitride surface layer on the sapphire which sets the N-face polarity of the growth.

NH₃ and Trimethylaluminum (TMA) are then flowed into the reactor to commence growth of a thin AlN layer in a step-flow-growth-mode or layer-by-layer growth mode. To increase the surface mobility of Al-species, a surfactant, for example indium, in form of trimethylindium (TMI), can be additionally flowed into the reactor [5].

Trimethylgallium (TMG) is then also flowed into the reactor to commence the growth of a graded or stepped Al_(x)Ga_(1-x)N layer, the composition of which is graded or stepped from AlN to GaN. The injection of TMI can be continued.(step optional)

NH₃ and Trimethylgallium are then flowed into the reactor to commence growth of the main GaN layer.

Currently, the growth method being used is MOCVD; however this invention could become quite useful for other growth methods such as MBE, HVPE, CBE, etc.

The process described applies very generally to GaN growth however, the invention can be easily utilized to create InN (with the use of TMI instead of TMG), AlN (with the use of TMA instead of TMG), or any of their alloys, also with other group-V atoms (Al, Ga, In)(N, P, As), by combining the appropriate precursors. Other precursors can be used such as triethylgallium, triethylaluminum for group-III sources, and dimethylhydrazine for N sources. Any appropriate substrate can be used, such as SiC, Si, spinel, etc. The nitridation temperature and time can be varied. Other growth initiation procedures can be applied. For example, the growth can be initiated with the deposition of an AlGaN layer etc., or no growth initiation step might be required at all. Note that, while part (b) specifies the deposition of a thin AlN layer, any thickness of the AlN layer may be used, and nitride materials other than AlN may be used. The annealing step of the substrate can be eliminated. The graded or stepped AlGaN layer can be eliminated and be replaced by any (Al, Ga, In)N layer of any composition if grown in a step-flow-growth-mode or layer-by-layer-growth-mode. The substrate can be misoriented not only towards the Si <−110> or Si <11-2> directions but also in any other direction. Misoriented Si (001) instead of Si(111) can be used as substrate. Instead of a single composition layer, the composition of the layer/crystal can be modified for all individual growth steps. The growth of each individual layer may also be interrupted for the deposition of layers comprised of other materials, for example silicon nitride or silicon oxide, possibly for strain or dislocation management.

FIG. 2B illustrates a process chart in accordance with the present invention.

Block 210 represents the step of placing a misoriented, chemo-mechanically polished (111) Si substrate in a MOCVD chamber.

Block 212 represents the step of annealing the misoriented Si substrate.

Block 214 represents the step of nitridizing the misoriented Si substrate.

Block 216 represents the step of depositing, on the nitridized misoriented substrate, a thin AlN layer in a step-flow or layer-by-layer growth mode.

Block 218 represents the optional step of introducing an additional Ga-precursor into the MOCVD chamber to deposit, on the AlN, a layer where the Al-composition is graded or stepped from AlN to GaN in a step-flow or layer by layer growth mode.

Block 220 represents the step of growing the main group III nitride layer on the graded layer.

Growth of Semi-Insulating Group-III Nitride Layers

For the growth of semi-insulating group-III nitride base layers a dopant with acceptor character, for example iron, possibly using the precursor bis-cyclopentadienyl-iron (Cp)₂Fe, is added during the growth of the layers or part of the layer growth, as seen in the process charts of FIGS. 3 and 4.

Devices utilizing lateral conduction, such as transistors, fabricated from group-III nitride heterostructures grown using this invention shall be aligned in such a way that the lateral carrier conduction occurs parallel to surface steps/undulations of the group-III nitride crystal. For example for layer structures deposited on sapphire with a misorientation direction of <11-20>, or on C-polar SiC substrates with a misorientation direction of <1-100>, both leading to group-III nitride surface steps/undulations parallel to the <11-20> direction of the GaN crystal, source and drain contacts of transistors need to be aligned in such a way that the transistor channel is aligned parallel to the <11-20> direction of the GaN crystal.

FIG. 3 illustrates a process chart in accordance with the present invention for the growth of semi-insulating GaN on sapphire.

Block 300 represents the step of placing a misoriented sapphire substrate in a MOCVD chamber.

Block 302 represents the step of annealing the misoriented sapphire substrate.

Block 304 represents the step of nitridizing the annealed misoriented sapphire substrate to form a thin (AlN surface layer) to set an N-polarity for following group-III nitride layers.

Block 306 represents the step of depositing, on the AlN, a group-III nitride nucleation layer in a step-flow or layer-by-layer growth mode, where either the entire layer or a part of the nucleation layer is doped with iron.

Block 308 represents the step of growing, on the AlN layer, the main group-III nitride layer, where either the entire layer or a part of the layer is doped with iron (the second group-III nitride layer having an N-face).

FIG. 4A illustrates a process chart in accordance with the present invention for the growth of semi-insulating GaN on a SiC substrate.

Block 400 represents the step of placing a misoriented, chemo-mechanically polished C-polar SiC substrate in a MOCVD chamber.

Block 402 represents the step of annealing the misoriented SiC substrate.

Block 404 represents the step of depositing, on the annealed substrate, a thin AlN layer in a step-flow or layer-by-layer growth mode where either the entire layer or a part of the layer is doped with iron.

Block 406 represents the optional step of introducing an additional Ga-precursor into the MOCVD chamber to deposit, on the AlN, a layer where the Al-composition is graded or stepped from AlN to GaN in a step-flow or layer by layer growth mode, where either the entire layer or a part of the layer is doped with iron.

Block 408 represents the step of growing, on the graded layer, the main group-III nitride layer where the entire layer or part of the layer are doped with iron (the group-III nitride layer having an N-face).

FIG. 4B illustrates a process chart in accordance with the present invention for the growth a Si (111) substrate.

Block 410 represents the step of placing a misoriented, chemo-mechanically polished Si substrate in a MOCVD chamber.

Block 412 represents the step of annealing the misoriented Si substrate.

Block 414 represents the step of nitridizing the misoriented Si substrate.

Block 416 represents the step of depositing, on the annealed substrate, a thin AlN layer in a step-flow or layer-by-layer growth mode where either the entire layer or a part of the layer is doped with iron.

Block 418 represents the optional step of introducing an additional Ga-precursor into the MOCVD chamber to deposit, on the AlN, a layer where the Al-composition is graded or stepped from AlN to GaN in a step-flow or layer by layer growth mode, where either the entire layer or a part of the layer is doped with iron.

Block 420 represents the step of growing, on the graded layer, the main group-III nitride layer where the entire layer or part of the layer are doped with iron (the first Group-III nitride layer having an N-face).

While the present invention, in FIGS. 3 to 4 for example, describes the growth of main group III-nitride layer(s), any nitride layers having an N-face may be grown, for example group III-V layers or group III-nitride layers having an N-face, as discussed throughout the specification.

Fe dopants can be replaced by other dopants with acceptor character, for example Mg, Zn or C.

The heteroepitaxially N-polar group-III nitride films grown according to the present invention serve as base layers for following group-III nitride layer sequences according to the specific device application.

FIG. 5( a) shows an optical microscope image of an N-face GaN film grown by MOCVD on a nitridized sapphire substrate. FIG. 5( b) shows an atomic force microscope (AFM) image of N-face GaN grown by MOCVD on a nitridized sapphire substrate, wherein the root mean square (RMS) roughness is 0.9 nm.

FIG. 6 shows transmission electron micrographs, under different imaging conditions, of an N-face GaN film grown using the present invention. The estimated threading dislocation density is at most of the order 10⁹ cm⁻².

FIG. 7( a) shows an AFM image of InGaN/GaN multi quantum wells (MQWs) grown using the present invention, where the RMS roughness is 0.85 nm, showing a smooth surface at InGaN growth temperatures. FIG. 7( b) shows 300 Kelvin photoluminescence (PL) of MQWs comprising 5×(3 nm thick In_(0.1)Ga_(0.9)N/8 nm thick GaN), grown by MOCVD according to the present invention.

FIG. 8 shows X-ray Diffraction (XRD) of N-face nitride MQWs comprising 5×(4 nm thick In_(0.12)Ga_(0.88)N/10 nm thick GaN), which is comparable to Ga-face XRD results.

Growth of p-Type N-Polar Group-III Nitrides

Similar to Ga-polar group-III nitrides, p-type doping can be executed using bis-cyclopentadienyl magnesium or one of its derivates as precursor. In N-polar nitride films, however, higher Mg doping levels can be realized without degradation of the crystal quality and the surface morphology. In addition, sharper Mg-doping profiles can be realized, realizing great advantages for a variety of p-n junction devices.

Stabilization of the Surface

To stabilize the surface of any N-polar group-III nitride film, a thin insulator layer, for example silicon nitride or silicon oxide, can be deposited on top of the nitride film, possibly in-situ. The surface can also be stabilized through the deposition of a thin p-type N-polar nitride film, which can be fabricated through doping with Mg using the precursor bis-cyclopentadienyl-magnesium, for example.

Growth of Group-III Nitrides with Surface Planes Comprised of a High Fraction of N Atoms

The use of misoriented substrates is beneficial also for the growth of group-III nitride films with surfaces which are comprised of a high fraction of N atoms other than the (000-1) surface, for example semi-polar N-face films.

Impurity Incorporation in Heteroepitaxial N-Face and Ga-Face GaN Grown by MOCVD.

In group III-nitrides, the crystal growth orientation has a substantial impact upon the chemical and physical properties of the material. Among these properties is the impurity incorporation, which has been studied on Ga-face (0001) GaN, but has not been extensively explored for N-face (000-1) GaN. Presumably, the discrepancy in the understanding between the two polarities arises from the historically rough hexagonal surface morphology of N-face GaN when grown by MOCVD. However, the present invention has shown that through the use of vicinal sapphire substrates, smooth N-face GaN can be grown heteroepitaxially by MOCVD. As such, surface roughnesses and threading dislocations grown on misoriented substrates, as shown in the present invention, are comparable to Ga-face GaN films.

The present invention has also studied the difference in impurity incorporation between MOCVD grown N-face GaN on different sapphire off-cuts, and Ga-face GaN, using secondary ion mass spectroscopy (SIMS). The unintentional impurities oxygen, carbon, and hydrogen, as well as the intentional impurities silicon and magnesium, were studied as a function of changes in the temperature, pressure, V/III ratio and Ga flow.

Ga-face and N-face GaN templates, approximately 1 μm thick, were first grown separately, due to the need for different growth initiation conditions. For the N-face, templates were grown on off-cuts of 2°, 4°, 5° towards the sapphire [10-10] direction as well as 4° and 5° towards the sapphire [11-20] direction. A piece of the Ga-face and each of the N-face templates were then co-loaded in the MOCVD reactor, where a “SIMS stack” was regrown which allowed a direct comparison between each of the off-cuts and polarities. The first SIMS stack explored variations in Ga flow and pressure, while the second contained variations in temperature and V/III ratio.

The SIMS results for oxygen incorporation as a function of temperature, shown in FIG. 9, indicated that oxygen incorporation on all of the N-face off-cuts was substantially higher than the Ga-face. However, the carbon incorporation as a function of temperature, shown in FIG. 10, was substantially higher on the Ga-face when compared to all of the N-face off-cuts. Models based upon the difference in atomic bonding on N-/Ga-face surfaces will be presented elsewhere. Additionally, the impact of changes in the growth conditions for oxygen and carbon incorporation will be discussed elsewhere. Hydrogen incorporation was comparable between both polarities. The present invention found that Mg and Si incorporation was also comparable on all samples.

However, the present invention found a significant difference in the Mg incorporation profiles, between N- and Ga-face samples, as shown in FIG. 11. These results present a direct comparison between the impurity incorporation of Ga- and N-face GaN films, and indicate that impurity incorporation on smooth N-face can be controlled through growth conditions for use in device applications. P-type (e.g. Mg) doping N-face nitride films leads to the creation of abrupt p-type doping profiles, as evidenced by the profile 1100 in FIG. 11( a), as compared to the less well defined p-type doping profiles 1102 produced when p-type doping Ga-face nitride films. Thus, the present invention provides a method for the creating a group III-nitride film with an abrupt p-type doping profile, comprising growing and doping a group III-nitride film with an N-face.

Advantages and Improvements

Currently most N-polar GaN films grown by MOCVD, which is the most commonly used growth method for large scale fabrication of GaN based devices, are characterized by large (μm sized) hexagonal features which make the material unacceptable for device applications. This invention allows for the growth of smooth, high quality films which makes the development of N-face devices possible.

For HEMTs, device structures which were not feasible with the traditional Ga-face will now be available with smooth N-face growth.

One of the major challenges to III-Nitride based light emitters is the growth of high quality InGaN. N-face allows the growth of InGaN at higher temperatures than the traditional Ga-face, which provides better quality material as well as making higher indium content films feasible [6].

Another challenge to the growth of light emitters is p-type doping. In the traditional Ga-face material, too high p-type doping (Mg) causes the surface to locally invert to N-face causing a poor quality film. Since the growth is now performed on the N-face the film quality can be maintained at higher levels of p-type doping which will lead to a much better device performance. In addition sharper Mg-doping profiles can be realized further improving the device performance.

III-Nitride based light emitters suffer from strong polarization induced electric fields. N-face material provides an electric field in the opposite direction to the traditional Ga-face which should allow, for instance, for lower operating voltages and improved carrier injection resulting in an increased efficiency in light emitting devices.

The etching properties of N-face are distinctly different from that of Ga-face which will be useful in creating better light extraction schemes in LEDs, such as surface roughening, and mega-cones, as well as etched facets for LDs.

The Mg memory effect, present on Ga-face, is not significant on the N-face, which allows for the creation of abrupt p-type doping profiles, not available on the Ga-face, for use in device structures.

N-polar devices grown on misoriented substrates make use of enhanced charge (e.g. electron and/or hole) transport properties in a specific direction related to the misorientation direction through appropriate alignment of the device channel with respect to the misorientation direction. So, for example, and not by way of limitation, the channel of a transistor or charge transport channel of any device can be created such that the orientation of the channel and the enhanced charge transport properties are both used to create the desired charge transport for a given device. Some devices may desire faster charge transport, and, as such, the channel would be aligned perpendicular to the misorientation direction of the N-face (Al, Ga, In)N layer(s) to increase charge transport in such devices; other devices may require a resistance or other slowing of the charge transport, and the channel can be aligned parallel or at some other alignment other than parallel to the enhanced charge transport of the misoriented N-face film grown on the misoriented substrate. Such design characteristics can now be taken into account when designing the device which were previously unavailable to the device designer.

FIGS. 12 a-12 f illustrate optical micrographs of 0.8 micron thick GaN films grown on sapphire substrates in accordance with the present invention.

FIG. 12 a shows growth in a misorientation of 0.5 degrees towards the a-plane, and FIG. 12 b shows growth in a misorientation of 0.5 degrees toward the m-plane.

FIG. 12 c shows growth in a misorientation of 1 degree towards the a-plane, and FIG. 12 d shows growth in a misorientation of 1 degree toward the m-plane.

FIG. 12 e shows growth in a misorientation of 2 degrees towards the a-plane, and FIG. 12 f shows growth in a misorientation of 2 degrees toward the m-plane.

The inserts in FIGS. 12 a and 12 b are enlarged 3 times from that of the main figures.

Growth of Additional Group-III Nitride Layers and

Additional Methods for Growing N-polar Group-III Nitride Layers

The present invention also includes methods for growing N-polar (N-face) III-nitride layers, i.e., layers oriented in an N-polar direction, where the N-polarity of the layer is not established at the onset of the epitaxial growth of the III-Nitride layers, but rather in a later stage of growth. Specifically, on a given misoriented substrate, first a III-polar (i.e., Ga-polar) III-nitride layer is grown or deposited. Then a transition layer is grown or deposited, followed by deposition or growth of an N-polar III-nitride layer on top of the transitional layer. The atomic structure of the surface of the transition layer which is adjacent to the N-polar III-nitride layer is designed so that III-N layers subsequently grown atop the transition layer are oriented in the N-polar direction. In some embodiments, the portion of the transition layer adjacent to the Ga-polar III-nitride layer is Ga-polar, the portion of the transition layer furthest from the Ga-polar III-nitride layer is N-polar, the polarity of the layer transitions from Ga-polar to N-polar in between, and all III-N materials grown on top of the transition layer are oriented in the N-polar direction. The transition layer converting the polarity can be comprised of a heavily doped group-III nitride layer, in particular with magnesium or zinc, or a thin magnesium nitride or zinc nitride layer, or other dopants.

FIG. 13 illustrates one or more embodiments of the present invention that incorporate such growth.

Substrate 1300 is shown, with a misoriented growth surface 1302. Again, the misorientation can be in any direction, but the misorientation angle is typically between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices. If the substrate is [111] silicon, such a method optionally comprises a misorientation with a misorientation direction of <−1-12>, the miller indices of the misorientation direction are h=−1, k=−1 and l=2 or equivalent, or a misorientation direction of <11-2>, the miller indices of the misorientation direction are h=1, k=1 and l=−2 or equivalent.

A Group-III polar layer 1304 is then grown on the substrate. The layer 1304 is typically a gallium-polar layer, but can be other Group-III polarities without departing from the scope of the present invention. In some embodiments, the thickness of layer 1304 is about 1 nanometer to 10 micron, such as about 10 nanometers to 1 micron. In some embodiments, layer 1304 comprises a single Ga-polar III-N material, while in other embodiments layer 1304 includes two or more Ga-polar III-N materials. On top of layer 1304 is grown a transition layer 1306. This can be done by growing a Group-III Nitride layer which is heavily doped with magnesium ([Mg]≧6×10¹⁹ cm⁻³), typically with a thickness of 0.1 to 2 μm, [9] or by growing a thin, typically 0.1-2 nm thick magnesium nitride layer, [10] or both. The transition layer 1306 can be comprised of or include other elements and compounds, such as one or more layers of aluminum, aluminum carbide, aluminum oxide, low-temperature aluminum nitride, boron, boron nitride, boron carbide, boron oxide, silicon, silicon carbide, silicon nitride, silicon oxide, iron, iron nitride, iron oxide, or gallium oxide, or other materials, or layers in combination with low-temperature gallium nitride or aluminum nitride, which will all either convert the polarity of the transition layer 1306 from a group-III polarity to an N-polarity, or result in the growth of an N-polar Group-III Nitride layer 1308 on top of the transition layer 1306.

The N-polar III-nitride layer 1308 can have any dopant profile desired. For example, if an N-polar Al_(x)Ga_(1-x)N film is desired for layer 1308, such a film can be grown on layer 1306 without including magnesium or other dopants present in the transition layer 1306. Additional N-polar III-nitride layers can be deposited or grown on top of layer 1308. The group-III polar layer 1304, the transition layer 1306 and any other layers in the structure can be also doped with iron to render them semi-insulating.

Substrate Misorientation

FIGS. 14A-14C are micrographs of N-polar films grown on various substrates in accordance with one or more embodiments of the present invention.

FIG. 14A illustrates an N-polar GaN film on a (111) silicon substrate without a misorientation angle, i.e., the growth surface of the substrate is in the (111) plane. Feature 1400 is a hexagonal defect, several of which appear on the upper surface of the GaN film. The surfaces of feature 1400 do not lie in the same plane as the remainder of the GaN surface. Thus, additional layers or films grown on such a layer will have additional cracks, threading dislocations, or other undesirable features, such that devices cannot be made from such layers or films. As such, device-quality films or layers cannot be fabricated.

FIG. 14B illustrates an N-polar GaN film on a silicon substrate with a misorientation angle of 3.5 degrees toward the (11-2) plane, i.e., the growth surface of the substrate is 3.5 degrees away from the (111) plane toward the (11-2) plane. The surface of the GaN no longer comprises feature 1400. As such, device-quality films or layers can be fabricated on such a layer, and such layers can be smoother, or have a better surface quality, than those layers or films grown on substrates without misorientation angles.

FIG. 14C illustrates an N-polar GaN film on a silicon substrate with a misorientation angle of 3.5 degrees toward the (1-10) plane, i.e., the growth surface of the substrate is 3.5 degrees away from the (111) plane toward the (1-10) plane. The surface of the GaN no longer comprises feature 1400. As such, device-quality films or layers can be fabricated on such a layer. Again, such a layer is smoother, or has a better surface quality, than a layer grown on a substrate without a misorientation angle.

As such, a preferred misorientation direction for silicon is typically 3.5 degrees toward the (11-2) plane from the (111) plane, but other misorientation angles or directions are still possible with a silicon substrate. Other substrates may have different misorientation angles, and such substrates and misorientation angles are also within the scope of the present invention.

FIGS. 15A-B are atomic force microscope (AFM) images of GaN surfaces showing surface topologies.

FIG. 15A is an AFM image of the GaN surface of FIG. 14B, indicating a 0.8 nm Root Mean Square (RMS) surface roughness.

FIG. 15B is an AFM image of a different portion of the GaN surface of FIG. 14B, indicating a 2 nm Root Mean Square (RMS) surface roughness.

FIGS. 16A-B are transmission electron micrograph (TEM) images of GaN films produced by one or more embodiments of the present invention.

FIG. 16A shows threading dislocations 1600 within the GaN film 1602. The GaN film 1602 comprises the structure shown in FIG. 17. FIG. 16B is a Convergent Beam Electron Diffraction (CBED) micrograph of the structure in FIG. 16A which confirms the N-polarity of GaN film 1602. Spot 1604 shows a (000-2) plane, spot 1606 shows a (000) plane, and spot 1608 shows a (0002) plane of the GaN film 1602.

The structure in FIG. 17 includes substrate 1700, which is a misoriented (111) silicon substrate that is misoriented 3.5 degrees away from the (111) plane in the (11-2) direction. Layer 1702 is a III-nitride film, that begins as AlN at surface 1704 and is graded to GaN at the surface adjacent to layer 1706. The portion of layer 1702 adjacent to substrate 1700 is oriented in a Ga-polar direction. Layer 1706 is a GaN layer. When GaN layer 1706 is doped, the polarity of overlying layers can be converted to N-polarity. GaN layer 1706 is typically doped with magnesium, but other elements can be used to convert the polarity within the scope of the present invention. Layers 1702 and 1706 can be rendered semi-insulating by additionally doping them with iron or other dopants that result in semi-insulating III-N materials.

Polarity conversion can occur in either of the two layers 1702 or 1706. For example, layer 1702 can be grown without any doping, and polarity conversion is achieved by Mg doping of layer 1706. Alternately, if layer 1702 is doped, the polarity can convert within layer 1702, and layer 1706 can be eliminated. Layer 1708 can be an unintentionally doped N-polar GaN layer, and layer 1602 can be a GaN layer doped with silicon or other dopants.

The estimated threading dislocation density in the layer 1602 is on the order of 10⁹ cm⁻², which can be small enough to enable the formation of devices. Other epitaxial techniques such as molecular beam epitaxy or chloride vapor phase epitaxy can be used to fabricate the layers.

REFERENCES

The following references are incorporated by reference herein:

[1] Homo-epitaxial GaN growth on exact and misoriented single crystals: suppression of hillock formation: A. R. A. Zauner, J. L. Weyher, M. Plomp, V. Kirilyuk, I. Grzegory, W. J. P. van Enckevort, J. J. Schermer, P. R. Hageman, and P. K. Larsen, J. Cryst. Growth 210 (2000) 435-443.

[2] Homo-epitaxial GaN growth on the N-face of GaN single crystals: the influence of the misorientation on the surface morphology: A. R. A. Zauner, A. Aret, W. J. P. van Enckevort, J. L. Weyher, S. Porowski, J. J. Schermer, J. Cryst. Growth 240 (2002) 14-21.

[3] A. P. Grzegorczyk et al. Influence of sapphire annealing in trimethylgallium atmosphere on GaN epitaxy by MOCVD: J. Cryst. Growth 283 (2005) 72-80.

[4] N-polarity GaN on sapphire substrates grown by MOCVD: T. Matsuoka, Y. Kobayashi, H. Takahata, T. Mitate, S Mizuno, A. Sasaki, M. Yoshimoto, T. Ohnishi, and M. Sumiya, Phys. Stat. Sol. (b) 243 (2006) 1446-1450.

[5] Indium-surfactant-assisted growth of high-mobility AlN/GaN multilayer structures by MOCVD, S. Keller, S. Heikman, I. Ben-Yaakov, L. Shen, S. P. DenBaars, and U. K. Mishra, Appl. Phys. Lett. 79 (2001) 3449.

[6] The effect of substrate polarity on the growth of InN by RF-MBE: Naoi et al., J. Cryst. Growth 269 (2004) 155-161.

[7] Nitridation of sapphire. Effect on the optical properties of GaN epitaxial overlayers: N. Grandjean, J. Massies, and M. Leroux, Appl. Phys. Lett. 69 (1996) 2071.

[8] Energetics of AlN thin films on the Al₂O₃ (0001) surface: R. Di Felice and J. Northrup, Appl. Phys. Lett. 73 (1998) 936.

[9] The growth of N-face GaN by MOCVD: effect of Mg, Si, and In: P. R. Travernier, T. Margalith, J. Williams, D. S. Green, S. Keller, S. P. DenBaars, U. K. Mishra, S. Nakamura, and D. R. Clarke, J. Cryst. Growth 264 (2004) 150.

[10] Control of the polarity of GaN films using an Mg adsorption layer: N. Grandjean, A. Dussaigne, S. Pessagna, and P. Vennegues, J. Cryst. Growth 251 (2003) 460.

CONCLUSION

This concludes the description of the preferred embodiment of the present invention. The foregoing description of one or more embodiments of the invention has been presented for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed. Many modifications and variations are possible in light of the above teaching. It is intended that the scope of the invention be limited not by this detailed description, but rather by the claims appended hereto and the full range of equivalents to the claims appended hereto. 

1. A method for forming an N-polar group III-nitride layer, comprising: obtaining a growth surface of a substrate, wherein the growth surface has a misorientation angle between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices; growing a group III-nitride layer on the growth surface, wherein the group III-nitride layer has an orientation other than an N-polar [000-1] orientation; growing a transition layer on the group III-nitride layer, wherein the transition layer establishes an N-polar [000-1] orientation for one or more subsequent layers grown on the transition layer; and growing an N-polar group III-nitride layer on the transition layer, wherein the N-polar group III-nitride layer has the N-polar [000-1] orientation established by the transition layer.
 2. A method for forming an N-polar group III-nitride layer, comprising: obtaining a growth surface of a substrate, wherein the growth surface has a misorientation angle between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, l are miller indices; growing a group III-polar III-nitride layer on the growth surface; growing a transition layer on the group III-polar III-nitride layer, wherein the transition layer establishes an N-polar [000-1] orientation for one or more subsequent layers grown on the transition layer; and growing an N-polar group III-nitride layer on the transition layer, wherein the N-polar group III-nitride layer has the N-polar [000-1] orientation established by the transition layer.
 3. The method of claim 1, further including inserting one or more additional group III-polar III-nitride layers between the substrate and the transition layer.
 4. The method of claim 2, wherein the N-polar group III-nitride layer is smoother than an N-polar group III-nitride layer grown on a substrate without a misorientation angle in the substrate's growth surface.
 5. The method of claim 2, wherein the transition layer is doped with magnesium.
 6. The method of claim 2, wherein a portion of the transition layer adjacent to a first surface of the transition layer is Ga-polar and a portion of the transition layer adjacent to a second surface of the transition layer is N-polar.
 7. The method of claim 6, wherein the first surface is adjacent to the group III-polar III-nitride layer and the second surface is adjacent to the N-polar group III-nitride layer.
 8. The method of claim 2, further including growing one or more additional N-polar III-nitride layers on top of the N-polar group III-nitride layer to form an N-face transistor or light emitting device structure.
 9. The method of claim 2, wherein the miller indices are h=1, i=0, k=0 and l=−1 and the substrate is silicon carbide.
 10. The method of claim 2, wherein the miller indices are h=0, i=0, k=0 and l=1 and the substrate is sapphire.
 11. The method of claim 2, wherein the miller indices are h=1, k=1, l=1 and the substrate is silicon.
 12. The method of claim 2, wherein the substrate is (001) Si.
 13. The method of claim 2, wherein the growing is by Metal Organic Chemical Vapor Deposition (MOCVD).
 14. The method of claim 2, wherein the substrate is a nitridized misoriented substrate.
 15. The method of claim 1, wherein the N-polar group III-nitride layer is smoother than an N-polar group III-nitride layer grown on a substrate without a misorientation angle in the growth surface.
 16. The method of claim 1, wherein the transition layer is doped with magnesium.
 17. The method of claim 1, wherein the miller indices are h=1, i=0, k=0 and l=−1 and the substrate is silicon carbide.
 18. The method of claim 1, wherein the miller indices are h=0, i=0, k=0 and l=1 and the substrate is sapphire.
 19. The method of claim 1, wherein the miller indices are h=1, k=1, l=1 and the substrate is silicon.
 20. The method of claim 1, wherein the substrate is (001) Si.
 21. The method of claim 1, wherein the growing is by Metal Organic Chemical Vapor Deposition (MOCVD).
 22. The method of claim 1, wherein the substrate is a nitridized misoriented substrate.
 23. A method for altering charge transport properties in a channel of a nitride device, comprising: fabricating the nitride device using N-face nitride layers grown on a transition layer which is grown on a substrate having a growth surface with a misorientation angle between 0.5 and 10 degrees relative to a miller indexed crystallographic plane [h, i, k, l] of the substrate, where h, i, k, and l are miller indices, wherein at least one of the N-face nitride layers is a misoriented N-face (Al,Ga,In)N layer, at least one of the N-face nitride layers includes the channel of the nitride device, and an atomic structure of a surface of the transition layer adjacent to the N-face nitride layers results in III-N layers grown on top of the transition layer being oriented in an N-polar direction; and orienting the channel of the nitride device with respect to a misorientation direction of the misoriented N-face (Al,Ga,In)N layer grown on the misoriented substrate to alter the charge transport properties of the channel.
 24. The method of claim 23, wherein the N-face nitride layers are smoother than N-face nitride layers grown on a substrate without a misorientation angle in the substrate's growth surface.
 25. The method of claim 23, wherein the transition layer is doped with magnesium.
 26. The method of claim 1, wherein an atomic structure of a surface of the transition layer adjacent to the N-polar group III-nitride layer results in the N-polar group III-nitride grown on top of the transition layer being oriented in an N-polar direction.
 27. The method of claim 1, wherein the group III-nitride layer is Ga-polar Gallium Nitride (GaN) and the N-polar group III-nitride layer is a GaN layer. 